| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186590066-186590335 | Rare:84 | ||||
| chr2:187448133-187448407 | Rare:43 | ||||
| chr2:188291672-188292066 | Common:4; Rare:108 | ||||
| chr2:188292716-188292861 | Common:1; Rare:38 | ||||
| chr2:188974203-188974284 | Rare:21 | ||||
| chr2:188974320-188974575 | Rare:64; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189007641-189007946 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr2:189441072-189441526 | Common:2; Rare:148 | ||||
| chr2:189580736-189580957 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783965-189784111 | Common:3; Rare:53; Clinvar (benign):1 | ||||
| chr2:189784294-189784532 | Common:4; Rare:84; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:190343880-190343923 | Rare:5 | ||||
| chr2:190343940-190344031 | Rare:20 | ||||
| chr2:190534688-190534919 | Common:1; Rare:74 | ||||
| chr2:190648703-190648923 | Common:1; Rare:81 |